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Diagnostic Cervical Conization for Persistent Infection or Integration of HPV

A Study of the Value of Diagnostic Cervical Conization for Persistent Infection or Integration of Human Papillomavirus

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05510830
Enrollment
250
Registered
2022-08-22
Start date
2022-10-31
Completion date
2030-01-31
Last updated
2022-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Cancer, Cervical Conization, Cervical Intraepithelial Neoplasia, Human Papilloma Virus Infection, Human Papilloma Virus Integration

Keywords

HPV persistent infection, HPV integration, diagnostic cervical conization

Brief summary

For the patients with cervical persistent infection or integration of HPV, we has designed a program to perform cervical conization for certain patients to earlier and better diagnose and cure the diseases of HPV infection and related cervical intraepithelial neoplasia/cancer.

Detailed description

For the patients with cervical persistent infection or integration of human papillomavirus, the incidence of suffering cervical cancer or percancerous lesions increases. As the biopsy guided by colposcopy might miss some lesions, the cervical conization plays a role for the patients with high risk factors to diagnose the related cervical diseases. In this study, we has designed a program to perform cervical conization for certain patients to earlier and better diagnose and cure the diseases of HPV infection and related cervical intraepithelial neoplasia/cancer.

Interventions

PROCEDUREdiagnostic cervical conization

For the patients who met the inclusion criteria, the gynecologists perform cervical conization and pathological examinations. Then the patients will be followed-up for at least two years with the tests of cervical TCT & HPV, and colposcopy if necessary. The data will be analyzed and see if the patients with high risk factors benefit from the surgery or not.

Sponsors

National Natural Science Foundation of China
CollaboratorOTHER_GOV
Tongji Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. The patients are referred to colposcopy and biopsy examinations due to abnormal cervical screening results with no precancerous lesions discovered by pathology. 2. The cervical precancerous lesions are highly suspected by clinicians with one or more following risk factors: * The course of HPV type 16/18 persistent infection is more than two years. * The integration reads of HPV is more than 15. * The impression of colposcopy indicates precancerous lesions. * The cervical TCT indicates ASC-H/HSIL/SCC/AGC-FN/AIS/AC.

Exclusion criteria

1. Pregnant women. 2. Vaginal intraepithelial neoplasia is highly suspected by colposcopy and pathological examinations. 3. The patients are suffering malignant tumors of other system and have not been cured. 4. There is acute inflammation of the lower genital or anal tract. 5. The patients' health will be severely harmed by the colposcopy and cervical conization due to some circumstances such as severe insufficiency of liver and kidney function, blood diseases and acute inflammation of other systems.

Design outcomes

Primary

MeasureTime frameDescription
The incidence of discovering concealed cervical cancer or percancerous lesionsup to 2 months after recruitedThe pathological examinations of the cervical conization might discover some concealed cervical cancer or precancerous lesions which could not be discovered by biopsy guided by colposcopy.
The incidence of HPV clearance after the cervical conizationThrough the study completion, an average of 3~5 yearsAfter the cervical conizations, the patients will be arranged for follow-up every six months and HPV will be tested to see if the virus is cleared or not

Countries

China

Contacts

Primary ContactShuang Li, M.D
lee5190008@126.com18971625668
Backup ContactDongli Kong, M.D
kongdongli1988@163.com15107173860

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026